Genome-Wide Association Study Reveals Multiple Loci Influencing Normal Human Facial Morphology von Shaffer, John R, Orlova, Ekaterina, Lee, Myoung Keun, Leslie, Elizabeth J, Raffensperger, Zachary D, Heike, Carrie L, Cunningham, Michael L, Hecht, Jacqueline T, Kau, Chung How, Nidey, Nichole L, Moreno, Lina M, Wehby, George L, Murray, Jeffrey C, Laurie, Cecelia A, Laurie, Cathy C, Cole, Joanne, Ferrara, Tracey, Santorico, Stephanie, Klein, Ophir, Mio, Washington, Feingold, Eleanor, Hallgrimsson, Benedikt, Spritz, Richard A, Marazita, Mary L, Weinberg, Seth M

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Directed differentiation of human pluripotent cells to neural crest stem cells von Menendez, Laura, Kulik, Michael J, Page, Austin T, Park, Sarah S, Lauderdale, James D, Cunningham, Michael L, Dalton, Stephen

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Microtia: Epidemiology and genetics von Luquetti, Daniela V., Heike, Carrie L., Hing, Anne V., Cunningham, Michael L., Cox, Timothy C.

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Robin sequence: from diagnosis to development of an effective management plan von Evans, Kelly N, Sie, Kathleen C, Hopper, Richard A, Glass, Robin P, Hing, Anne V, Cunningham, Michael L

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De novo mutations in SMCHD1 cause Bosma arhinia microphthalmia syndrome and abrogate nasal development von Gordon, Christopher T, Xue, Shifeng, Yigit, Gökhan, Filali, Hicham, Chen, Kelan, Rosin, Nadine, Yoshiura, Koh-ichiro, Oufadem, Myriam, Beck, Tamara J, McGowan, Ruth, Magee, Alex C, Altmüller, Janine, Dion, Camille, Thiele, Holger, Gurzau, Alexandra D, Nürnberg, Peter, Meschede, Dieter, Mühlbauer, Wolfgang, Okamoto, Nobuhiko, Varghese, Vinod, Irving, Rachel, Sigaudy, Sabine, Williams, Denise, Ahmed, S Faisal, Bonnard, Carine, Kong, Mung Kei, Ratbi, Ilham, Fejjal, Nawfal, Fikri, Meriem, Elalaoui, Siham Chafai, Reigstad, Hallvard, Bole-Feysot, Christine, Nitschké, Patrick, Ragge, Nicola, Lévy, Nicolas, Tunçbilek, Gökhan, Teo, Audrey S M, Cunningham, Michael L, Sefiani, Abdelaziz, Kayserili, Hülya, Murphy, James M, Chatdokmaiprai, Chalermpong, Hillmer, Axel M, Wattanasirichaigoon, Duangrurdee, Lyonnet, Stanislas, Magdinier, Frédérique, Javed, Asif, Blewitt, Marnie E, Amiel, Jeanne, Wollnik, Bernd, Reversade, Bruno

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Transcriptomic Signatures of Single-Suture Craniosynostosis Phenotypes von Lapehn, Samantha, Gustafson, Jonas A, Timms, Andrew E, Cunningham, Michael L, Paquette, Alison G

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Calvarial osteoblast gene expression in patients with craniosynostosis leads to novel polygenic mouse model von Gustafson, Jonas A, Park, Sarah S, Cunningham, Michael L

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Modes of Action and Species-Specific Effects of Di-(2-ethylhexyl)Phthalate in the Liver von Rusyn, Ivan, Peters, Jeffrey M., Cunningham, Michael L.

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The 3D Facial Norms Database: Part 1. A Web-Based Craniofacial Anthropometric and Image Repository for the Clinical and Research Community von Weinberg, Seth M., Raffensperger, Zachary D., Kesterke, Matthew J., Heike, Carrie L., Cunningham, Michael L., Hecht, Jacqueline T., Kau, Chung How, Murray, Jeffrey C., Wehby, George L., Moreno, Lina M., Marazita, Mary L.

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A genome-wide association study identifies susceptibility loci for nonsyndromic sagittal craniosynostosis near BMP2 and within BBS9 von Justice, Cristina M, Yagnik, Garima, Kim, Yoonhee, Peter, Inga, Jabs, Ethylin Wang, Erazo, Monica, Ye, Xiaoqian, Ainehsazan, Edmond, Shi, Lisong, Cunningham, Michael L, Kimonis, Virginia, Roscioli, Tony, Wall, Steven A, Wilkie, Andrew O M, Stoler, Joan, Richtsmeier, Joan T, Heuzé, Yann, Sanchez-Lara, Pedro A, Buckley, Michael F, Druschel, Charlotte M, Mills, James L, Caggana, Michele, Romitti, Paul A, Kay, Denise M, Senders, Craig, Taub, Peter J, Klein, Ophir D, Boggan, James, Zwienenberg-Lee, Marike, Naydenov, Cyrill, Kim, Jinoh, Wilson, Alexander F, Boyadjiev, Simeon A

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Whole genome sequencing identifies associations for nonsyndromic sagittal craniosynostosis with the intergenic region of BMP2 and noncoding RNA gene LINC01428 von Musolf, Anthony M., Justice, Cristina M., Erdogan-Yildirim, Zeynep, Goovaerts, Seppe, Cuellar, Araceli, Shaffer, John R., Marazita, Mary L., Claes, Peter, Weinberg, Seth M., Li, Jae, Senders, Craig, Zwienenberg, Marike, Simeonov, Emil, Kaneva, Radka, Roscioli, Tony, Di Pietro, Lorena, Barba, Marta, Lattanzi, Wanda, Cunningham, Michael L., Romitti, Paul A., Boyadjiev, Simeon A.

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A randomized crossover trial comparing the Nifty cup to a medicine cup in preterm infants who have difficulty breastfeeding at Komfo Anokye Teaching Hospital (KATH) in Kumasi, Ghan... von McKinney, Christy M, Plange-Rhule, Gyikua, Ansong, Daniel, Cunningham, Michael L, Agyeman, Irene, Coffey, Patricia S

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Outcomes of Prenatal Antidepressant Exposure von Simon, Gregory E., Cunningham, Michael L., Davis, Robert L.

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A genome-wide association study implicates the BMP7 locus as a risk factor for nonsyndromic metopic craniosynostosis von Justice, Cristina M., Cuellar, Araceli, Bala, Krithi, Sabourin, Jeremy A., Cunningham, Michael L., Crawford, Karen, Phipps, Julie M., Zhou, Yan, Cilliers, Deirdre, Byren, Jo C., Johnson, David, Wall, Steven A., Morton, Jenny E. V., Noons, Peter, Sweeney, Elizabeth, Weber, Astrid, Rees, Katie E. M., Wilson, Louise C., Simeonov, Emil, Kaneva, Radka, Yaneva, Nadezhda, Georgiev, Kiril, Bussarsky, Assen, Senders, Craig, Zwienenberg, Marike, Boggan, James, Roscioli, Tony, Tamburrini, Gianpiero, Barba, Marta, Conway, Kristin, Sheffield, Val C., Brody, Lawrence, Mills, James L., Kay, Denise, Sicko, Robert J., Langlois, Peter H., Tittle, Rachel K., Botto, Lorenzo D., Jenkins, Mary M., LaSalle, Janine M., Lattanzi, Wanda, Wilkie, Andrew O. M., Wilson, Alexander F., Romitti, Paul A., Boyadjiev, Simeon A.

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Auriculocondylar syndrome 2 results from the dominant-negative action of PLCB4 variants von Kanai, Stanley M, Heffner, Caleb, Cox, Timothy C, Cunningham, Michael L, Perez, Francisco A, Bauer, Aaron M, Reigan, Philip, Carter, Cristan, Murray, Stephen A, Clouthier, David E

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Case-control study of neurodevelopment in deformational plagiocephaly von Speltz, Matthew L, Collett, Brent R, Stott-Miller, Marni, Starr, Jacqueline R, Heike, Carrie, Wolfram-Aduan, Antigone M, King, Darcy, Cunningham, Michael L

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Quantitative trait loci affecting the 3D skull shape and size in mouse and prioritization of candidate genes in-silico von Maga, A Murat, Navarro, Nicolas, Cunningham, Michael L, Cox, Timothy C

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Heterozygous mutations of FREM1 are associated with an increased risk of isolated metopic craniosynostosis in humans and mice von Vissers, Lisenka E L M, Cox, Timothy C, Maga, A Murat, Short, Kieran M, Wiradjaja, Fenny, Janssen, Irene M, Jehee, Fernanda, Bertola, Debora, Liu, Jia, Yagnik, Garima, Sekiguchi, Kiyotoshi, Kiyozumi, Daiji, van Bokhoven, Hans, Marcelis, Carlo, Cunningham, Michael L, Anderson, Peter J, Boyadjiev, Simeon A, Passos-Bueno, Maria Rita, Veltman, Joris A, Smyth, Ian, Buckley, Michael F, Roscioli, Tony

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Mutation discovery in mice by whole exome sequencing von Fairfield, Heather, Gilbert, Griffith J, Barter, Mary, Corrigan, Rebecca R, Curtain, Michelle, Ding, Yueming, D'Ascenzo, Mark, Gerhardt, Daniel J, He, Chao, Huang, Wenhui, Richmond, Todd, Rowe, Lucy, Probst, Frank J, Bergstrom, David E, Murray, Stephen A, Bult, Carol, Richardson, Joel, Kile, Benjamin T, Gut, Ivo, Hager, Jorg, Sigurdsson, Snaevar, Mauceli, Evan, Di Palma, Federica, Lindblad-Toh, Kerstin, Cunningham, Michael L, Cox, Timothy C, Justice, Monica J, Spector, Mona S, Lowe, Scott W, Albert, Thomas, Donahue, Leah Rae, Jeddeloh, Jeffrey, Shendure, Jay, Reinholdt, Laura G

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Genetic associations and phenotypic heterogeneity in the craniosynostotic rabbit von Gilbert, James R, Losee, Joseph E, Mooney, Mark P, Cray, James J, Gustafson, Jennifer, Cunningham, Michael L, Cooper, Gregory M

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